Method for identifying cancer drug candidates in Drosophila

ABSTRACT

A process for preparing information that identifies a compound as capable of perturbing the epithelium in a  D. melanogaster  comprising the steps of: i) obtaining a  D. melanogaster  which is genetically unmodified except that the  D. melanogaster  optionally comprises at least one nucleotide sequence encoding a reporter polypeptide operably linked to a promoter of an endogenous protein; ii) contacting the  D. melanogaster  with the compound; and iii) determining whether there is a difference between the epithelium of the  D. melanogaster  of ii) and the epithelium of a corresponding  D. melanogaster  not contacted with the compound, wherein the presence of a difference between the epithelium of the  D. melanogaster  contacted with the compound and the epithelium of a corresponding  D. melanogaster  not contacted with the compound identifies the compound as a compound that is capable of perturbing the epithelium in a  D. melanogaster.

This application claims the benefit of U.S. Provisional Application No. 61/561,560, filed Nov. 18, 2011, the contents of which are hereby incorporated by reference in their entirety.

This application incorporates-by-reference nucleotide and/or amino acid sequences which are present in the file named “121116_7526_83099_A_Sequence_Listing_REB.txt,” which is 107 kilobytes in size, and which was created Nov. 16, 2012 in the IBM-PC machine format, having an operating system compatibility with MS-Windows, which is contained in the text file filed Nov. 16, 2012 as part of this application.

Throughout this application, various publications are referenced, including referenced in parenthesis. Full citations for publications referenced in parenthesis may be found listed in alphabetical order at the end of the specification immediately preceding the claims. The disclosures of all referenced publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains.

BACKGROUND OF INVENTION

High Throughput Drug Screens

The drug discovery process has traditionally been initiated by searching a very large chemical library for compounds that can affect disease characteristics, to identify “hit” compounds. Hits are further tested and developed into leads. Lead compounds in turn are further refined, generally using medicinal chemistry, and tested with view to enter clinical trials and finally developing a drug for use in man.

High throughput screening methods for hits are generally based on in vitro cell culture, biochemical assays or receptor binding assays. Hit compounds identified in these assays need much in the way of further testing and refinement for in vivo use. Even in vitro cell culture assays, which are less artificial than biochemical or receptor binding assays, often fail to reliably indicate, for example, whether a compound will be toxic in vivo. The behavior of individual cells in culture can differ dramatically from the behavior of tissues in response to the same agent. Cells in culture often lack the nutrients, cell-cell contacts, basal membrane contacts, cell-cell signaling events, and physical forces that influence their behavior in vivo. Furthermore, immortalized cell lines often exhibit metabolisms and signal transduction events that vary markedly from the primary cell lines from which they are derived. As a result, the vast majority of hit compounds identified using traditional in vitro high throughput screening methods never become drugs, even after extensive medicinal chemistry optimization efforts are applied (Keserü and Makara, 2006).

In Vivo Drug Screens

Recently, there has been an increased interest in using whole animals to screen large chemical libraries. Such screens could potentially yield hits in a context in which relevant biological systems are present and functioning together in an intact organism. Though screens in mammalian models such as mice and rats are not practical due to the time and costs that would invariably be involved, smaller organisms whose biology has already been established to be relevant with respect to human disease are attractive candidates for use in drug discovery.

Drosophila melanogaster as a Tool for Drug Screens

The fruit fly (D. melanogaster) is a model organism which has been applied to the study of human genetics and development due to its small size, short generation time, prolific reproduction, and genetic tractability (Beir E., 2005). D. melanogaster's usefulness as a genetic tool has facilitated the development of high throughput in vivo screens for chemical suppressors of pathological phenotypes in genetically modified strains (e.g., U.S. Pat. No. 6,316,690). While such screens may provide lead compounds which have been identified in an in vivo context, they rely on flies with artificial genetic backgrounds that often do not develop or behave like wild-type flies. In addition, D. melanogaster is an invertebrate, and as a result many aspects of its development, metabolism, and morphology can be markedly different from those of mammals.

SUMMARY OF THE INVENTION

The present invention provides a process for preparing information that identifies a compound as capable of perturbing the epithelium in a D. melanogaster comprising the steps of:

-   i) obtaining at least one D. melanogaster which is genetically     unmodified except that the D. melanogaster optionally comprises at     least one nucleotide sequence encoding a reporter polypeptide     operably linked to a promoter of an endogenous protein; -   ii) contacting the at least one D. melanogaster with the compound;     and -   iii) determining whether there is a difference between the     epithelium of the at least one D. melanogaster of ii) and the     epithelium of a corresponding at least one D. melanogaster not     contacted with the compound,     wherein the presence of a difference between the epithelium of the     at least one D. melanogaster contacted with the compound and the     epithelium of a corresponding at least one D. melanogaster not     contacted with the compound identifies the compound as a compound     that is capable of perturbing the epithelium in a D. melanogaster.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; and -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the at least one egg chamber contacted with the     compound and the follicular epithelium of a corresponding at least     one egg chamber not contacted with the compound identifies the     compound as an epithelial cancer drug candidate.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound, wherein the     presence of a difference between the follicular epithelium of the at     least one egg chamber contacted with the compound and the follicular     epithelium of the corresponding at least one egg chamber not     contacted with the compound identifies the compound as an epithelial     cancer drug; and -   iv) producing the compound identified in step iii), thereby     producing the epithelial cancer drug.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound, and     up to four additional compounds; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and up to four additional compounds and the follicular     epithelium of a corresponding at least one egg chamber not contacted     with the compound and up to four additional compounds; -   iv) if there is a difference between the follicular epithelium of     the at least one egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of the     corresponding at least one egg chamber not contacted with the     compound, contacting at least one additional egg chamber according     to step i) with the compound but not the additional compound or     compounds of step ii) and step iii); and -   v) determining whether there is a difference between the follicular     epithelium of the at least one additional egg chamber of step iv)     and the follicular epithelium of a corresponding at least one     additional egg chamber not contacted with the compound,     -   wherein the presence of a difference between the follicular         epithelium of the at least one additional egg chamber of iv) and         the follicular epithelium of the corresponding at least one         additional egg chamber not contacted with the compound         identifies the compound as an epithelial cancer drug candidate.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound, and     up to four additional compounds; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and up to four additional compounds and the follicular     epithelium of a corresponding at least one egg chamber not contacted     with the compound and up to four additional compounds; -   iv) if there is a difference between the follicular epithelium of     the at least one egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of the     corresponding at least one egg chamber not contacted with the     compound, contacting at least one additional egg chamber according     to step i) with the compound but not the additional compound or     compounds of step ii) and step iii); and -   v) determining whether the there is a difference between the     follicular epithelium of the at least one additional egg chamber of     step iv) and the follicular epithelium of the corresponding at least     one additional egg chamber not contacted with the compound, wherein     the presence of a difference between the follicular epithelium of     the at least one additional egg chamber of step iv) and the     follicular epithelium of the corresponding at least one additional     egg chamber not contacted with the compound identifies the compound     as an epithelial cancer drug; and -   vi) producing the compound identified in step v), thereby producing     the epithelial cancer drug.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound; and -   iv) observing whether there is substantially more toxicity among     cells other than follicle cells of the at least one egg chamber     contacted with the compound than in the corresponding at least one     egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the at least one egg chamber contacted with the     compound and the follicular epithelium of the corresponding at least     one egg chamber not contacted with the compound, without the     presence of substantially more toxicity among cells other than     follicle cells of the at least one egg chamber contacted with the     compound than in the corresponding at least one egg chamber not     contacted with the compound, identifies the compound as an     epithelial cancer drug candidate.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) preparing or obtaining a group of compounds to be screened; -   ii) performing a process of the invention for each compound from the     group of compounds to identify an epithelial cancer drug candidate;     and -   iii) producing the compound identified in step ii), thereby     producing the epithelial cancer drug.

The present invention provides a process of preparing an epithelial cancer drug comprising:

-   i) preparing or obtaining a group of compounds to be screened; -   ii) performing a process of the invention for each compound from the     group of compounds to identify an epithelial cancer drug candidate; -   iii) producing the compound identified in step ii), thereby     producing the epithelial cancer drug; and -   iv) preparing the identified epithelial cancer drug candidate for     use in treating an epithelial cancer.

The present invention provides novel drug screening processes in D. melanogaster that overcome limitations of previous approaches.

The present invention provides a process for preparing information that identifies a compound as capable of perturbing the epithelium in a D. melanogaster comprising the steps of:

-   i) obtaining a D. melanogaster which is genetically unmodified     except that the D. melanogaster optionally comprises at least one     nucleotide sequence encoding a reporter polypeptide operably linked     to a promoter of an endogenous protein; -   ii) contacting the D. melanogaster with the compound; and -   iii) determining whether there is a difference between the     epithelium of the D. melanogaster of ii) and the epithelium of a     corresponding D. melanogaster not contacted with the compound,     wherein the presence of a difference between the epithelium of     the D. melanogaster contacted with the compound and the epithelium     of a corresponding D. melanogaster not contacted with the compound     identifies the compound as a compound that is capable of perturbing     the epithelium in a D. melanogaster.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; and -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound,     wherein the presence of a difference between the follicular     epithelium of an egg chamber contacted with the compound and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound identifies the compound as an epithelial cancer     drug candidate.

Aspects of the present invention provide a process of producing an epithelial cancer drug comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound, wherein the presence of a difference between the     follicular epithelium of an egg chamber contacted with the compound     and the follicular epithelium of a corresponding egg chamber not     contacted with the compound identifies the compound as an epithelial     cancer drug; and -   iv) producing the compound identified in step iii), thereby     producing the epithelial cancer drug.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound, and up to four     additional compounds; -   iii) determining whether there is a difference between follicular     epithelium of the egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of an egg     chamber not contacted with the compound and up to four additional     compounds; -   iv) if there is a difference between the follicular epithelium of     the egg chamber contacted with the compound and up to four     additional compounds and the follicular epithelium of an egg chamber     not contacted with the compound, contacting at least one additional     egg chamber according to step i) with the compound but not the     additional compound or compounds of step ii) and step iii); and -   v) determining whether there is a difference between the follicular     epithelium of the egg chamber of step iv) and the follicular     epithelium of an egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the egg chamber of iv) and the follicular epithelium     of an egg chamber not contacted with the compound identifies the     compound as an epithelial cancer drug candidate.

Aspects of the present invention provide a process of producing an epithelial cancer drug comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound, and up to four     additional compounds; -   iii) determining whether there is a difference between follicular     epithelium of the egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of an egg     chamber not contacted with the compound and up to four additional     compounds; -   iv) if there is a difference between the follicular epithelium of     the egg chamber contacted with the compound and up to four     additional compounds and the follicular epithelium of an egg chamber     not contacted with the compound, contacting at least one additional     egg chamber according to step i) with the compound but not the     additional compound or compounds of step ii) and step iii); and -   v) determining whether the there is a difference between the     follicular epithelium of the egg chamber of step iv) and the     follicular epithelium of an egg chamber not contacted with the     compound, wherein the presence of a difference between the     follicular epithelium of the egg chamber of step iv) and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound identifies the compound as an epithelial cancer     drug; and -   vi) producing the compound identified in step v), thereby producing     the epithelial cancer drug.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound; and -   iv) observing whether there is more toxicity among cells other than     follicle cells of the egg chamber contacted with the compound than     in the egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of an egg chamber contacted with the compound and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound, without the presence of substantially more     toxicity among cells other than follicle cells of the egg chamber     contacted with the compound than in the egg chamber not contacted     with the compound, identifies the compound as an epithelial cancer     drug candidate.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a process for preparing information that identifies a compound as capable of perturbing the epithelium in a D. melanogaster comprising the steps of:

-   i) obtaining at least one D. melanogaster which is genetically     unmodified except that the D. melanogaster optionally comprises at     least one nucleotide sequence encoding a reporter polypeptide     operably linked to a promoter of an endogenous protein; -   ii) contacting the at least one D. melanogaster with the compound;     and -   iii) determining whether there is a difference between the     epithelium of the at least one D. melanogaster of ii) and the     epithelium of a corresponding at least one D. melanogaster not     contacted with the compound,     wherein the presence of a difference between the epithelium of the     at least one D. melanogaster contacted with the compound and the     epithelium of a corresponding at least one D. melanogaster not     contacted with the compound identifies the compound as a compound     that is capable of perturbing the epithelium in a D. melanogaster.

In some embodiments, the process further comprises identifying whether a compound that is capable of perturbing the epithelium in a D. melanogaster specifically perturbs the epithelium by determining whether there is a difference between non-epithelial tissue of the at least one D. melanogaster contacted with the compound and the non-epithelial tissue of a corresponding at least one D. melanogaster not contacted with the compound, wherein when there is no difference between the non-epithelial tissue of the at least one D. melanogaster contacted with the compound and the non-epithelial tissue of a corresponding at least one D. melanogaster not contacted with the compound, the compound is identified as a compound that specifically perturbs the epithelium in a D. melanogaster.

In some embodiments, the at least one D. melanogaster comprises at least one nucleotide sequence encoding a reporter polypeptide operably linked to a promoter of an endogenous protein, and the reporter polypeptide is part of a fusion protein which comprises the endogenous protein.

In some embodiments, the endogenous protein is atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATJ, Lin-7, beta-catenin, or Armadillo (Arm).

In some embodiments, the endogenous protein is Par6.

In some embodiments, the at least one D. melanogaster is an at least one D. melanogaster embryo.

In some embodiments, contacting the at least one D. melanogaster embryo with the compound comprises injecting the compound into the at least one D. melanogaster embryo.

In some embodiments, the at least one D. melanogaster is an at least one female D. melanogaster, and the epithelium is the follicular epithelium of an egg chamber of the at least one female D. melanogaster.

In some embodiments, a compound which perturbs or specifically perturbs the epithelium in a D. melanogaster is an epithelial cancer drug candidate.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; and -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the at least one egg chamber contacted with the     compound and the follicular epithelium of a corresponding at least     one egg chamber not contacted with the compound identifies the     compound as an epithelial cancer drug candidate.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound, wherein the     presence of a difference between the follicular epithelium of the at     least one egg chamber contacted with the compound and the follicular     epithelium of the corresponding at least one egg chamber not     contacted with the compound identifies the compound as an epithelial     cancer drug; and -   iv) producing the compound identified in step iii), thereby     producing the epithelial cancer drug.

In some embodiments, the at least one D. melanogaster egg chamber comprises at least one nucleotide sequence encoding a reporter polypeptide operably linked to a promoter of an endogenous protein, and the reporter polypeptide is part of a fusion protein which comprises the endogenous protein.

In some embodiments, the endogenous protein is atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATJ, Lin-7, beta-catenin, or Armadillo (Arm).

In some embodiments, the endogenous protein is Par6.

In some embodiments, the difference between the follicular epithelium of the at least one egg chamber contacted with the compound and the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound is altered expression of the fusion protein in the follicular epithelium.

In some embodiments, altered expression of the fusion protein comprises increased expression of the fusion protein in the follicular epithelium of the at least one egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises decreased expression of the fusion protein in the follicular epithelium of the at least one egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises a different localization of the fusion protein within follicle epithelial cells of the at least one egg chamber contacted with the compound compared to follicle epithelial cells of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, there is proportionally less localization of the fusion protein at the apical side of the follicle epithelial cells of the at least one egg chamber contacted with the compound compared to the follicle epithelial cells of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises a different location of protein production and/or post-transcriptional modification of the fusion protein in the follicular epithelium of the at least one egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, the difference between the follicular epithelium of the at least one egg chamber contacted with the compound and the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound is altered architecture of the follicular epithelium of the at least one egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, the altered architecture comprises multilayering of follicle cells.

In some embodiments, the altered architecture comprises a change in the shape of a subtype of follicle cells.

In some embodiments, the difference between the follicular epithelium of the at least one egg chamber contacted with the compound and the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound is altered migration of a subtype of follicle cells within the follicular epithelium of the at least one egg chamber contacted with the compound compared to the same subtype of follicle cells within the follicular epithelium of the corresponding at least one egg chamber not contacted with the compound.

In some embodiments, the subtype of follicle cells is selected from the group consisting of border cells, stretch cells, polar cells, and centripetal cells.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound, and     up to four additional compounds; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and up to four additional compounds and the follicular     epithelium of a corresponding at least one egg chamber not contacted     with the compound and up to four additional compounds; -   iv) if there is a difference between the follicular epithelium of     the at least one egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of the     corresponding at least one egg chamber not contacted with the     compound, contacting at least one additional egg chamber according     to step i) with the compound but not the additional compound or     compounds of step ii) and step iii); and -   v) determining whether there is a difference between the follicular     epithelium of the at least one additional egg chamber of step iv)     and the follicular epithelium of a corresponding at least one     additional egg chamber not contacted with the compound,     -   wherein the presence of a difference between the follicular         epithelium of the at least one additional egg chamber of iv) and         the follicular epithelium of the corresponding at least one         additional egg chamber not contacted with the compound         identifies the compound as an epithelial cancer drug candidate.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound, and     up to four additional compounds; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and up to four additional compounds and the follicular     epithelium of a corresponding at least one egg chamber not contacted     with the compound and up to four additional compounds; -   iv) if there is a difference between the follicular epithelium of     the at least one egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of the     corresponding at least one egg chamber not contacted with the     compound, contacting at least one additional egg chamber according     to step i) with the compound but not the additional compound or     compounds of step ii) and step iii); and -   v) determining whether the there is a difference between the     follicular epithelium of the at least one additional egg chamber of     step iv) and the follicular epithelium of the corresponding at least     one additional egg chamber not contacted with the compound, wherein     the presence of a difference between the follicular epithelium of     the at least one additional egg chamber of step iv) and the     follicular epithelium of the corresponding at least one additional     egg chamber not contacted with the compound identifies the compound     as an epithelial cancer drug; and -   vi) producing the compound identified in step v), thereby producing     the epithelial cancer drug.

The present invention provides a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining at least one D. melanogaster egg chamber which is     genetically unmodified except that the at least one D. melanogaster     egg chamber optionally comprises at least one nucleotide sequence     encoding a reporter polypeptide operably linked to a promoter of an     endogenous protein; -   ii) contacting the at least one egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the at least one egg chamber contacted with     the compound and the follicular epithelium of a corresponding at     least one egg chamber not contacted with the compound; and -   iv) observing whether there is substantially more toxicity among     cells other than follicle cells of the at least one egg chamber     contacted with the compound than in the corresponding at least one     egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the at least one egg chamber contacted with the     compound and the follicular epithelium of the corresponding at least     one egg chamber not contacted with the compound, without the     presence of substantially more toxicity among cells other than     follicle cells of the at least one egg chamber contacted with the     compound than in the corresponding at least one egg chamber not     contacted with the compound, identifies the compound as an     epithelial cancer drug candidate.

In some embodiments, the presence of substantially more toxicity is observed in all cells other than follicle cells of the at least one egg chamber.

In some embodiments, the presence of substantially more toxicity is observed in one or more nurse cells of the at least one egg chamber.

In some embodiments, the presence of substantially more toxicity is observed in the oocyte of the at least one egg chamber.

In some embodiments, toxicity is determined by morphology.

In some embodiments, toxicity is increased cell death.

In some embodiments, the presence of more cell death is due to apoptosis.

In some embodiments, the presence of more cell death is due to necrosis.

In some embodiments, 10 to 30 D. melanogaster egg chambers are obtained and contacted with the compound.

In some embodiments, about 10, 15, 20, 25, or 30 D. melanogaster egg chambers are obtained and contacted with the compound.

In some embodiments, at least 10, 15, 20, 25, or 30 D. melanogaster egg chambers are obtained and contacted with each compound.

In some embodiments, 20 D. melanogaster egg chambers are obtained and contacted with the compound.

The present invention provides a process of producing an epithelial cancer drug comprising:

-   i) preparing or obtaining a group of compounds to be screened; -   ii) performing a process of the invention for each compound from the     group of compounds to identify an epithelial cancer drug candidate;     and -   iii) producing the compound identified in step ii), thereby     producing the epithelial cancer drug.

The present invention provides a process of preparing an epithelial cancer drug comprising:

-   i) preparing or obtaining a group of compounds to be screened; -   ii) performing a process of the invention for each compound from the     group of compounds to identify an epithelial cancer drug candidate; -   iii) producing the compound identified in step ii), thereby     producing the epithelial cancer drug; and -   iv) preparing the identified epithelial cancer drug candidate for     use in treating an epithelial cancer.

In some embodiments, a process of the invention is performed for each compound in at least one well of a microwell plate, wherein the microwell plate has multiple wells such that a process of the invention may be performed for more than one compound from the group of compounds using the microwell plate.

In some embodiments, a process of the invention is performed for more than one compound from the group of compounds using the microwell plate.

In some embodiments, 10 to 30 D. melanogaster egg chambers are obtained and contacted with each compound.

In some embodiments, about 10, 15, 20, 25, or 30 D. melanogaster egg chambers are obtained and contacted with each compound.

In some embodiments, at least 10, 15, 20, 25, or 30 D. melanogaster egg chambers are obtained and contacted with each compound.

In some embodiments, 20 D. melanogaster egg chambers are obtained and contacted with each compound.

The present invention provides a process for preparing information that identifies a compound as capable of perturbing the epithelium in a D. melanogaster comprising the steps of:

-   i) obtaining a D. melanogaster which is genetically unmodified     except that the D. melanogaster optionally comprises at least one     nucleotide sequence encoding a reporter polypeptide operably linked     to a promoter of an endogenous protein; -   ii) contacting the D. melanogaster with the compound; and -   iii) determining whether there is a difference between the     epithelium of the D. melanogaster of ii) and the epithelium of a     corresponding D. melanogaster not contacted with the compound,     wherein the presence of a difference between the epithelium of     the D. melanogaster contacted with the compound and the epithelium     of a corresponding D. melanogaster not contacted with the compound     identifies the compound as a compound that is capable of perturbing     the epithelium in a D. melanogaster.

In some embodiments the process further comprises identifying whether a compound that is capable of perturbing the epithelium in a D. melanogaster specifically perturbs the epithelium by determining whether there is a difference between non-epithelial tissue of the D. melanogaster contacted with the compound and the non-epithelial tissue of a corresponding D. melanogaster not contacted with the compound, wherein when there is no difference between the non-epithelial tissue of the D. melanogaster contacted with the compound and the non-epithelial tissue of a corresponding D. melanogaster not contacted with the compound, the compound is identified as a compound that specifically perturbs the epithelium in a D. melanogaster.

In some embodiments, the D. melanogaster comprises at least one nucleotide sequence encoding a reporter polypeptide operably linked to a promoter of an endogenous protein, and the reporter polypeptide is part of a fusion protein which comprises the endogenous protein.

In some embodiments, the endogenous protein is atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATJ, Lin-7, beta-catenin, or Armadillo (Arm).

In some embodiments, the endogenous protein is Par6.

In some embodiments, the D. melanogaster is a D. melanogaster embryo.

In some embodiments, contacting the D. melanogaster embryo with the compound comprises injecting the compound into the D. melanogaster embryo.

In some embodiments, the D. melanogaster is a female D. melanogaster, and the epithelium is the follicular epithelium of an egg chamber of the female D. melanogaster.

In some embodiments, a compound which perturbs or specifically perturbs the epithelium in a D. melanogaster is an epithelial cancer drug candidate.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; and -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound,     wherein the presence of a difference between the follicular     epithelium of an egg chamber contacted with the compound and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound identifies the compound as an epithelial cancer     drug candidate.

Aspects of the present invention provide a process of producing an epithelial cancer drug comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound, wherein the presence of a difference between the     follicular epithelium of an egg chamber contacted with the compound     and the follicular epithelium of a corresponding egg chamber not     contacted with the compound identifies the compound as an epithelial     cancer drug; and -   iv) producing the compound identified in step iii), thereby     producing the epithelial cancer drug.

In some embodiments, the D. melanogaster egg chamber comprises at least one nucleotide sequence encoding a reporter polypeptide operably linked to a promoter of an endogenous protein, and the reporter polypeptide is part of a fusion protein which comprises the endogenous protein.

In some embodiments, the endogenous protein is atypical kinase C (aPKC), Par3, Part, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATJ, Lin-7, beta-catenin, or Armadillo (Arm).

In some embodiments, the endogenous protein is Par6.

In some embodiments, the difference between the follicular epithelium of an egg chamber contacted with the compound and the follicular epithelium of a corresponding egg chamber not contacted with the compound is altered expression of the fusion protein in follicular epithelium.

In some embodiments, altered expression of the fusion protein comprises increased expression of the fusion protein in follicular epithelium of the egg chamber contacted with the compound compared to the follicular epithelium of a corresponding egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises decreased expression of the fusion protein in follicular epithelium of the egg chamber contacted with the compound compared to follicular epithelium of a corresponding egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises a different localization of the fusion protein within follicle epithelial cells of the egg chamber contacted with the compound compared to follicle epithelial cells of a corresponding egg chamber not contacted with the compound.

In some embodiments, there is proportionally less localization of the fusion protein at the apical side of the follicle epithelial cells of the egg chamber contacted with the compound compared to follicle epithelial cells of a corresponding egg chamber not contacted with the compound.

In some embodiments, altered expression of the fusion protein comprises a different location of protein production and/or post-transcriptional modification of the fusion protein in the follicular epithelium of the egg chamber contacted with the compound compared to the follicular epithelium of a corresponding egg chamber not contacted with the compound.

In some embodiments, the difference between the follicular epithelium of an egg chamber contacted with the compound and the follicular epithelium of an egg chamber not contacted with the compound is altered architecture of the follicular epithelium compared to the follicular epithelium a corresponding egg chamber not contacted with the compound.

In some embodiments, the altered architecture comprises multilayering of follicle cells.

In some embodiments, the altered architecture comprises a change in the shape of a subtype of follicle cells.

In some embodiments, the difference between the follicular epithelium of an egg chamber contacted with the compound and the follicular epithelium of an egg chamber not contacted with the compound is altered migration of a subtype of follicle cells within the follicular epithelium compared to the same subtype of follicle cells within the follicular epithelium an egg chamber not contacted with the compound.

In some embodiments, the subtype of follicle cells is selected from the group consisting of border cells, stretch cells, polar cells, and centripetal cells.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound, and up to four     additional compounds; -   iii) determining whether there is a difference between follicular     epithelium of the egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of an egg     chamber not contacted with the compound and up to four additional     compounds; -   iv) if there is a difference between the follicular epithelium of     the egg chamber contacted with the compound and up to four     additional compounds and the follicular epithelium of an egg chamber     not contacted with the compound, contacting at least one additional     egg chamber according to step i) with the compound but not the     additional compound or compounds of step ii) and step iii); and -   v) determining whether there is a difference between the follicular     epithelium of the egg chamber of step iv) and the follicular     epithelium of an egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of the egg chamber of iv) and the follicular epithelium     of an egg chamber not contacted with the compound identifies the     compound as an epithelial cancer drug candidate.

Aspects of the present invention provide a process of producing an epithelial cancer drug comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound, and up to four     additional compounds; -   iii) determining whether there is a difference between follicular     epithelium of the egg chamber contacted with the compound and up to     four additional compounds and the follicular epithelium of an egg     chamber not contacted with the compound and up to four additional     compounds; -   iv) if there is a difference between the follicular epithelium of     the egg chamber contacted with the compound and up to four     additional compounds and the follicular epithelium of an egg chamber     not contacted with the compound, contacting at least one additional     egg chamber according to step i) with the compound but not the     additional compound or compounds of step ii) and step iii); and -   v) determining whether the there is a difference between the     follicular epithelium of the egg chamber of step iv) and the     follicular epithelium of an egg chamber not contacted with the     compound, wherein the presence of a difference between the     follicular epithelium of the egg chamber of step iv) and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound identifies the compound as an epithelial cancer     drug; and

vi) producing the compound identified in step v), thereby producing the epithelial cancer drug.

Aspects of the present invention provide a process for preparing information that identifies whether a compound is an epithelial cancer drug candidate comprising:

-   i) obtaining a D. melanogaster egg chamber which is genetically     unmodified except that the D. melanogaster egg chamber optionally     comprises at least one nucleotide sequence encoding a reporter     polypeptide operably linked to a promoter of an endogenous protein; -   ii) contacting the egg chamber with the compound; -   iii) determining whether there is a difference between the     follicular epithelium of the egg chamber contacted with the compound     and the follicular epithelium of an egg chamber not contacted with     the compound; and -   iv) observing whether there is more toxicity among cells other than     follicle cells of the egg chamber contacted with the compound than     in the egg chamber not contacted with the compound,     wherein the presence of a difference between the follicular     epithelium of an egg chamber contacted with the compound and the     follicular epithelium of a corresponding egg chamber not contacted     with the compound, without the presence of substantially more     toxicity among cells other than follicle cells of the egg chamber     contacted with the compound than in the egg chamber not contacted     with the compound, identifies the compound as an epithelial cancer     drug candidate.

In some embodiments, the presence of more toxicity is observed in all cells other than follicle cells of the egg chamber.

In some embodiments, the presence of more toxicity is observed in one or more nurse cells of the egg chamber.

In some embodiments, the presence of more toxicity is observed in the oocyte of the egg chamber.

In some embodiments, toxicity is determined by morphology.

In some embodiments, toxicity is increased cell death.

In some embodiments, the presence of more cell death is due to apoptosis.

In some embodiments, the presence of more cell death is due to necrosis.

Each embodiment disclosed herein is contemplated as being applicable to each of the other disclosed embodiments. Thus, all combinations of the various elements described herein are within the scope of the invention.

It is understood that where a parameter range is provided, all integers within that range, and tenths thereof, are also provided by the invention. For example, “0.2-5 mg/kg/day” is a disclosure of 0.2 mg/kg/day, 0.3 mg/kg/day, 0.4 mg/kg/day, 0.5 mg/kg/day, 0.6 mg/kg/day etc. up to 5.0 mg/kg/day.

Terms

As used herein, and unless stated otherwise, each of the following terms shall have the definition set forth below.

As used herein, “about” in the context of a numerical value or range means±10% of the numerical value or range recited or claimed, unless the context requires a more limited range.

As used herein, a “cancer drug candidate” is a compound which is identified to produce a difference in a D. melanogaster which has been contacted with the compound, compared to a D. melanogaster which has not been contacted with the compound.

As used herein, “epithelial cancer” means a carcinoma. A carcinoma is a cancer derived from epithelial cells. Subtypes of carcinomas include but are not limited to adenocarcinoma, squamous cell carcinoma, adenosquamous carcinoma, anaplastic carcinoma, large cell carcinoma, small cell carcinoma, giant cell carcinoma, spindle cell carcinoma, sarcomatoid carcinoma, pleomorphic carcinoma, carcinosarcoma, pulmonary blastoma, basal cell carcinoma, linitis plastica, vipoma, cholangiocarcinoma, hepatocellular carcinoma, adenoid cystic carcinoma, renal cell carcinoma, adnexal and skin appendage neoplasms, mucoepidermoid neoplasms, and acinar cell neoplasms. The term carcinoma encompasses lung cancers, liver cancers, ovarian cancers, brain cancers, breast cancers, prostate cancers, colon cancers, pancreatic cancers, and brain cancers, of epithelial origin.

As used herein, “D. melanogaster” refers to an insect or insects as well as to parts of the insect belonging to the species Drosophila melanogaster, without regard to the developmental stage thereof and including, embryos (eggs), larvae, pupae, and mature adult flies of the insect, unless a specific developmental stage or a specific part is specified.

As used herein in regard to cell and tissue function, to “perturb” means to alter an aspect of the normal cell and tissue function of an organism, including but not limited to the embryonic development of a D. melanogaster, the development of an epithelium within a D. melanogaster, the development of a structure or tissue within a D. melanogaster such as an egg chamber of a D. melanogaster, or the development of an epithelium within a part of a D. melanogaster, such as an egg chamber. To perturb cell and tissue function of an epithelium, may mean to alter the normal growth, behavior, or morphology of a cell or the progeny thereof that is within a developing epithelium, and/or to alter the normal interaction or arrangement of cells or the progeny thereof that are within a developing epithelium, and/or to alter the normal growth, behavior, or morphology of a developing epithelium. To “perturb the epithelium” means to alter an aspect of a normal epithelial cell's function or of an epithelial tissue function in an organism or a part thereof.

As used herein, “epithelium” refers to tissue that lines the cavities and surfaces of an organism's body, and also form many glands. Types of D. melanogaster epitheliums include but are not limited to the follicular epithelium of the egg chamber, and the blastoderm epithelium, foregut epithelium, hindgut epithelium, neuroectodermal endothelium, subperineurium and peripheral glia, gonadal sheet, dorsal vessel, salivary glands, and malpighian tubules of the embryo.

As used herein, “follicular epithelium” or “follicle cell epithelium” means the somatic monolayer which surrounds the germ cells of a Drosophila melanogaster egg chamber. The follicular epithelium produces yolk and eggshell components of the egg, and also participates in signaling events with the germ cells that help determine future embryonic axes (Horne-Badovinac and Bilder, 2005).

As used herein, “follicle cell” means a cell which is part of, or derived from the follicular epithelium.

As used herein, “label” means a substance which may be introduced into a living or non-living cell such that it allows for the specific detection of a protein within the cell by any technique known in the art. The label may comprise a portion that is capable of binding to another protein, and a portion that is a marker. In some aspects of the invention, the portion that is capable of binding to another protein is attached to the marker by a covalent bond.

As used herein, a “marker” may be any molecule that provides an identifiable signal within a cell, or that facilitates the determination of the expression or location of a protein in a cell by any technique known in the art. Non-limiting examples of markers are fluorescent dyes, phosphorescent dyes, quantum dots, and reporter polypeptides.

As used herein, a “reporter polypeptide” is a protein or oligopeptide that provides an identifiable signal within a cell, or which is capable of being specifically detected within a cell by any technique known in the art. The cell may be alive or dead. Examples of reporter polypeptides include but are not limited to streptavidin, beta-galactosidase, epitope tags, fluorescent proteins, luminescent proteins and chromogenic enzymes such as horseradish peroxidase.

As used herein, an “epitope tag” is an amino acid sequence for which antibodies with suitable specificity and affinity have been generated, or may be generated.

As used herein, “altered expression” means having an amount or localization of a protein in a cell which is or was contacted with at least one compound, or the progeny thereof, compared to amount of localization of the protein in a corresponding untreated cell, or the progeny thereof. Altered expression of a protein may be increased expression of the protein, decreased expression of the protein, or a different localization of the protein within a cell or the progeny of the cell that is or has been contacted with at least one compound compared to a corresponding untreated cell or the progeny thereof. Altered expression may also be a different location of expression of the protein within a group of cells or a tissue in a D. melanogaster which is or has been contacted with at least one compound, compared to a corresponding group of cells or tissue in an untreated D. melanogaster, for example, within the follicular epithelium of an egg chamber of a D. melanogaster.

As used herein, “altered architecture” means a different number, shape, and/or arrangement of cells within a group of cells or a tissue of a D. melanogaster which is or has been contacted with at least one compound compared to a corresponding group of cells or tissue in an untreated D. melanogaster. In one non-limiting example, altered architecture may be the multilayering of cells in a D. melanogaster which has been contacted with a compound in a location where the corresponding cells an untreated D. melanogaster form a monolayer.

As used herein, “incubation medium” means growth medium which contains a compound with which a D. melanogaster egg chamber will be contacted and/or is being contacted and/or was contacted.

As used herein, a “fluorophore” is a molecule which absorbs electromagnetic energy at one wavelength and re-emits energy at another wavelength. A fluorophore may be a molecule or part of a molecule including fluorescent dyes and proteins.

Labels, Markers, and Reporter Polypeptides

Aspects of the invention relate to the detection of a labeled protein or a fusion protein within a D. melanogaster. The label may be used to specifically detect the presence and/or the amount and/or the localization of any endogenous protein which is expressed in the epithelium of a D. melanogaster. The label may also be used to detect the presence of a fusion protein which is expressed in the epithelium of a D. melanogaster. The fusion protein may comprise amino acids in the sequence of the amino acid sequence of an endogenous protein melanogaster and the amino acid sequence of a reporter polypeptide. In some embodiments, the protein which is expressed in the epithelium of a wild-type D. melanogaster is atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATj, Lin-7, beta-catenin, or Armadillo (Arm). In some embodiments which comprise a label, the protein to which the label binds is Par6. In some embodiments which comprise a fusion protein, the fusion protein comprises amino acids in the amino acid sequence of Par6 and the amino acid sequence of a reporter polypeptide. The label may comprise a portion that is capable of binding to a protein or fusion protein, and a marker. The portion of the label which is capable of binding to a protein or fusion protein may be covalently attached to the marker.

One of skill in the art will understand that there may be more than one isoform for each of atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATj, Lin-7, beta-catenin, or Armadillo (Arm), and that any isoform of one of these proteins may be used in accordance with embodiments of the invention. Non-limiting examples of atypical kinase C (aPKC), Par3, Par6, Cdc42, DE-Cadherin, Crumbs (Crb), Stardust (Sdt), PATj, Lin-7, Armadillo (Arm) and beta-catenin isoform amino acid sequences are set forth as SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO: 12, and SEQ ID NO: 13, respectively.

In some embodiments which comprise a label, the label comprises a marker which is a fluorophore. Non-limiting examples of fluorophores include fluorescent dyes, phosphorescent dyes, quantum dots, xanthene derivatives, cyanine derivatives, naphthalene derivatives, coumarin derivatives, oxadiaxol derivatives, pyrene derivatives, acridine derivatives, arylmethine derivatives, tetrapyrrole derivatives. Xanthene derivatives include but are not limited to fluorescein, rhodamine, Oregon green, eosin, Texas red, and Cal Fluor dyes. Cyanine derivatives include but are not limited to cyanine, indocarbocyanine, oxacarbocyanine, thiacarbocyanine, merocyanine, and Quasar dyes. Naphthalene derivatives include but are not limited to dansyl and prodan derivatives. Oxadiazole derivatives include but are not limited to pyridyloxazol, nitrobenzoxadiazole and benzoxadiazole. A non-limiting example of a pyrene derivative is cascade blue. Oxadine derivatives include but are not limited to Nile red, Nile blue, cresyl violet, and oxazine 170. Acridine derivatives include but are not limited to proflavin, acridine orange, and acridine yellow. Arylmethine derivatives include but are not limited to auramine, crystal violet, and malachite green. Tetrapyrrole derivatives include but are not limited to porphin, phtalocyanine and bilirubin.

In some embodiments which comprise a label and a fusion protein, the label may comprise a portion that binds to the fusion protein and a marker. For instance, the fusion protein may comprise an epitope tag to which the label binds, wherein the label comprises an antibody fragment that binds to the epitope tag. In one embodiment, the fusion protein comprises streptavidin, and the portion of the label which binds to the fusion protein is biotin.

In some embodiments, the label comprises a marker which is a reporter polypeptide.

In aspects of the invention which comprise a fusion protein or a label which comprises a reporter polypeptide, the reporter polypeptide may be an epitope tag, a fluorescent protein, a luminescent protein, a chromogenic enzyme, streptavidin, beta-galactosidase, or any other reporter polypeptide as defined herein.

Examples of epitope tags include but are not limited to V5-tag, Myc-tag, HA-tag, FLAG-tag, GST-tag, and His-tags. Additional examples of epitope tags are described in the following references: Huang and Honda, CED: a conformational epitope database. BMC Immunology 7:7 biomedcentral.com/1471-2172/7/7#B1. Retrieved Feb. 16, 2011 (2006); and Walker and Rapley, Molecular biomethods handbook. Pg. 467 (Humana Press, 2008). These references in their entireties are hereby incorporated by reference into this application. In some embodiments of the invention a label comprising an antibody or an antibody fragment is used to detect the localization and/or expression of a fusion protein which comprises an epitope tag.

Fluorescent proteins will be well known to one skilled in the art, and include but are not limited to GFP, AcGFP, EGFP, TagGFP, EBFP, EBFP2, Asurite, mCFP, mKeima-Red, Azami Green, YagYFP, YFP, Topaz, mCitrine, Kusabira Orange, mOrange, mKO, TagGFP, RFP, DsRed, DsRed2, mstrawberry, mRFP1, mCherry, and, mRaspberry. Examples of luminescent proteins include but are not limited to enzymes which may catalyze a reaction that emits light, such as luciferase. Examples of chromogenic enzymes include but are not limited to horseradish peroxidase and alkaline phosphatase.

General techniques and compositions for detecting and/or observing and/or analyzing labels and/or fusion proteins which are useful in the present invention are described in the following references: Tsien et al., Fluorophores for confocal microscopy. Handbook of biological confocal microscopy. New York: Plenum Press, 1995; Rietdorf, Mocroscopic techniques. Advances in Biochemical Engineering/Biotechnology. Berlin: Springer 2005; Lakowicz, J R, Principles of fluorescence spectroscopy (3^(rd) ed.). Springer, 2006. These references in their entireties are hereby incorporated by reference into this application.

Injection of Compounds

Injected D. melanogaster embryos may be used to identify whether a compound is biologically active and/or a cancer drug candidate. In some embodiments, a compound that has biological activity perturbs the epithelium in a D. melanogaster. Unlabeled embryos or genetically modified embryos may be used. Use of a D. melanogaster embryo to test a compound for biological activity may comprise steps related to culturing D. melanogaster, embryo laying, embryo harvesting, embryo alignment, embryo injection, and embryo analysis to determine whether there is at least one difference between an embryo that has been injected with the compound and a embryo that has not been injected with the compound. General techniques useful for the culture and preparation of Drosophila include those described in the following references: Ashburner et al., Drosophila. A laboratory handbook. 1989, Cold Spring Harbor Laboratory Press, ISBN 0-87969-321-5, and Sullivan et al., ed., Drosophila Protocols. 2000, Cold Spring Harbor Laboratory Press, ISBN 978-087969586-6. These references in their entireties are hereby incorporated by reference into this application.

Fly Culture

In aspects of the invention which relate to fly culture and the injection of a compound into an embryo, at least one D. melanogaster adult female fly may be used to make a laying pot for embryo harvesting. The laying pot comprises a laying substrate plate. The D. melanogaster adult female fly may be 2-3 days old, 2-5 days old, or 2, 3, 4, or 5 days old. In some embodiments, it is necessary to wait until the D. melanogaster adult female fly has adapted to laying pot before collecting embryos. It may be necessary to wait at least 24 hours, or 24, 30, 36, 42, or 48 hours.

Embryo Laying

On the same day that at least one embryo is injected with a compound or compounds, the existing substrate plate is replaced with a new laying substrate plate in the laying pot, and the D. melanogaster adult female fly is given a period of time to lay retained, overdeveloped eggs. In some embodiments, the period of time given may be 1, 1.5, 2, 2.5, or 3 hours. The laying substrate plate containing overdeveloped eggs is then removed from the laying pot and incubated. The laying substrate plate may be incubated at a temperature of 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30° C. The laying substrate plate may be incubated for 45, 50, 55, 60, 65, 70, 75, 80, 85, or 90 minutes. In some embodiments, the laying substrate plate may be incubated for longer than 90 minutes.

Embryo Harvesting and Alignment

Some embodiments of the invention which encompass D. melanogaster embryo harvesting may comprise the steps of:

-   i) placing a basket strainer in a petri dish filled with 0.1%     Tween-20/H₂O; -   ii) harvesting the embryos from the laying substrate plate with a     brush wet with 0.1% Tween-20/H₂O, and adding them to the basket     strainer; -   iii) replacing the 0.1% Tween-20/H₂O from the petri dish, with a     dechorionation agent to remove the chorions of the embryos; -   iv) monitoring the dechorionation under a microscope; -   v) replacing the dechorionation agent with H₂O; -   vi) washing the embryos by replacing the H₂O with new H₂O; -   vii) drying the bottom of the basket; -   viii) removing the embryos with a spatula; -   ix) placing the embryos on a piece of agar; -   x) aligning the embryos; -   xi) preparing a slide with adhesive, and adhering the aligned     embryos to the adhesive by inverting the slide over the embryos; and -   xii) desiccating the embryos in a petri dish filled with silica gel.

Non-limiting examples of dechorionation agents which may be used in steps iii) and iv) are 25%, 30%, 35%, 40%, 45%, or 50% bleach in water. It will be understand that “H₂O” as used in steps i) to xii) hereinabove may include H₂O that comprises salts and/or buffers. In some embodiments, step vi) may be repeated 1, 2, 3, 4, 5, or 6 times, or more. In some embodiments, in the embryos of step x) may be aligned with their posterior poles in the same direction.

Injection of Embryos

Some embodiments of the invention which relate to injecting a compound into a D. melanogaster embryo may comprise the steps of:

-   i) filling a needle with a solution comprising the compound; -   ii) creating an opening at the tip of the needle; -   iii) adjusting the drop size exiting the needle to a desired amount     using a graticule; and -   iv) injecting the embryo through the posterior pole.

The desired amount of step iii) may be 50 to 500 pL, or about 50, 100, 150, 200, 250, 300, 350, 400, 450, or 500 pL. In some embodiments the desired amount is 420 pL.

Analysis

In some embodiments in which the embryo is not labeled and does not express a fusion protein, differences in embryos injected with a compound compared to embryos not injected with the compound may be determined by light microscopy. If embryos which are labeled or that express a fusion protein are used, the label or fusion protein may be observed by appropriate methodologies including but not limited to fluorescent and confocal microscopy. After an embryo is injected with a compound, the embryo may be processed for analysis using standard procedures. Which procedure is performed will depend on the label used or the fusion protein expressed in the embryo. In some embodiments of the invention, the embryo is incubated, stained, or otherwise contacted with a label, such that the label becomes attached to a protein within the embryo, before analysis of the embryo is performed.

Embryos may be observed for development and death. The embryos may be observed for 1-12 h. In some embodiments, the embryos are observed for 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 10.5, 11, 11.5, or 12 hours. In some embodiments, the death of an embryo after the embryo is injected with a compound may identify the compound as being a toxic compound.

Determining whether there is a difference between an embryo which has been injected with a compound and an embryo which has not been injected with the compound may be performed at any time point or time points occurring from the moment of injection of the compound until the embryo has developed into an adult fly. A time point may be a point of time as counted from a beginning reference point in time such as from the approximate moment of egg laying or the approximate moment of injection, or from any D. melanogaster developmental stage.

Soaking of Egg Chambers

Aspects of the invention relate to the use of a dissected D. melanogaster egg chamber to test a compound for biological activity, or to determine whether a compound is a cancer drug candidate. In some embodiments, a compound that has biological activity perturbs the epithelium in a D. melanogaster. Dissected egg chambers from wild-type D. melanogaster or from a genetically modified D. melanogaster may be used. In some embodiments of the invention the D. melanogaster may be genetically modified to express a fusion protein comprising amino acids in the sequence of the amino acid sequence of a protein which is naturally expressed in D. melanogaster, and a reporter polypeptide. In some embodiments, a label is used to detect the expression and/or localization of a protein in an egg chamber.

Processes of the invention which use a D. melanogaster egg chamber to test a compound for biological activity or to determine whether a compound is a cancer drug candidate may comprise steps related to culturing D. melanogaster, preparing D. melanogaster, dissection of an egg chamber or egg chambers from at least one D. melanogaster adult female fly, contacting the egg chamber or egg chambers with the compound, preparing the egg chamber for analysis, and analyzing the egg chamber for at least one difference between an egg chamber that has been contacted with the compound and a corresponding egg chamber that has not been contacted with the egg chamber. General techniques useful for the culture and preparation of D. melanogaster include those described in the following references: Ashburner et al., Drosophila. A laboratory handbook. 1989, Cold Spring Harbor Laboratory Press, ISBN 0-87969-321-5, and Sullivan et al., ed., Drosophila Protocols. 2000, Cold Spring Harbor Laboratory Press, ISBN 978-087969586-6. These references in their entireties are hereby incorporated by reference into this application.

Fly Culture

In some embodiments of the invention which relate to fly culture and the soaking of an egg chamber with a compound, at least one D. melanogaster adult female fly is incubated with at least one D. melanogaster adult male fly. In some embodiments, the D. melanogaster adult female fly may be 1 to 3 days old. In some embodiments, the D. melanogaster adult female fly is 1, 1.5, 2, 2.5, or 3 days old. In some embodiments, the D. melanogaster adult female fly may be incubated with at least one D. melanogaster adult male fly for 1 to 2 days. In some embodiments, the D. melanogaster adult female fly is incubated with at least one D. melanogaster adult male fly for 1, 1.5, or 2 days. In some embodiments, at least one D. melanogaster adult female fly is incubated with at least one D. melanogaster adult male fly in a bottle or vial containing D. melanogaster food and yeast ad libitum.

Fly Preparation

Some embodiments of the invention which relate to D. melanogaster adult female fly preparation may comprise the steps of:

-   1) selecting at least one D. melanogaster adult female fly on a CO₂     pad or after incubation of the D. melanogaster adult female fly at a     temperature that is sufficiently reduced to immobilize the D.     melanogaster adult female fly; -   ii) decapitating the D. melanogaster adult female fly; and -   iii) transferring the D. melanogaster adult female fly to a dish     which is cooled until the D. melanogaster a adult female fly is     dissected.

In some embodiments, the dish of step iii) is cooled to a temperature at 4° C. or less.

In some embodiments, the number of female flies selected is a number that is suitable for the number of compounds. In some embodiments, 10 to 30 female flies are selected for each compound. In some embodiments about 20 female flies are selected for each compound. In some embodiments, about 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50 female flies are selected for each compound. In some embodiments about 200, 400, 600, 800, or 1000 female flies are selected for about 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50 compounds.

Dissection

In some embodiments of the invention which encompass D. melanogaster adult female fly dissection may comprise the steps of:

-   i) removing the ovaries of at least one D. melanogaster adult female     fly for each compound; -   ii) placing the ovaries into growth medium; and -   iii) separating the ovarioles.

In some embodiments, the ovaries of 1-10 D. melanogaster adult female flies are removed. In some embodiments, the ovaries of 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 D. melanogaster adult female flies are removed.

The ovaries may be placed into 100-200 μL of growth medium, or about 100, 125, 150, 175, or 200 μL of growth medium. Examples of growth media which are suitable for use in embodiments of the invention include but are not limited to Shields and Sang M3 insect medium, Schneider's medium, Robb's medium (Theurkauf, W E, Chapter 25, Methods in Cell Biology Volume 44 (1994) Lawrence S. B. Goldstein and Eric A. Fyrberg, ISBN 978-0-12-564145-6) and others, all of which may or may not be supplemented with any combination of fetal bovine serum, albumin and/or other supplements. In some embodiments, the growth medium is not supplemented with fetal bovine serum. In some embodiments, the growth medium is not supplemented with a serum free supplement. In some embodiments, the growth medium is not supplemented with a growth factor. In some embodiments, the growth medium is not supplemented with a hormone. In some embodiments, the growth medium is supplemented with fetal bovine serum or a serum free supplement or a growth factor or a hormone, or any combination thereof.

The ovarioles are processed to remove the impact of muscle sheath contraction during analysis.

Some embodiments of the invention which encompass D. melanogaster adult female fly dissection may comprise the steps of:

-   i) Transferring flies to an electric liquefier filled with up to 250     mL of dissection medium. In some embodiments, the electric liquefier     is filled with about 100 to about 500 mL of dissection medium. In     some embodiments, the electric liquefier is filled with about 100,     150, 200, 250, 300, 350, 400, 450, or 500 mL of dissection medium.     Suitable dissection mediums include but are not limited to Shields     and Sang M3 insect medium, Schneider's medium, Robb's medium     (Theurkauf, W E, Chapter 25, Methods in Cell Biology Volume     44 (1994) Lawrence S. B. Goldstein and Eric A. Fyrberg, ISBN     978-0-12-564145-6) and others, all of which may or may not be     supplemented with any combination of fetal bovine serum, albumin     and/or other supplements. In some embodiments, the growth medium is     not supplemented with fetal bovine serum. In some embodiments, the     growth medium is not supplemented with a serum free supplement. In     some embodiments, the growth medium is not supplemented with a     growth factor. In some embodiments, the growth medium is not     supplemented with a hormone. In some embodiments, the growth medium     is supplemented with fetal bovine serum or a serum free supplement     or a growth factor or a hormone, or any combination thereof; -   ii) Isolating egg chambers by fly maceration in the electric     liquefier. In some embodiments, the egg chambers are isolated by fly     maceration in the electric liquefier with 1, 2, 3, 4, or 5 second     pulses repeated 1, 2, 3, 4, or 5 times in low speed. In some     embodiments, the egg chambers are isolated by fly maceration in the     electric liquefier with 2 second pulses repeated 3 times in low     speed; -   iii) Filtrating the fly homogenate through a mesh placed over a cup.     Isolated egg chambers pass through the mesh and unopened flies and     debris are retained in the mesh. In some embodiments, the cup is a     glass cup. The mesh may be made of steel, nylon, popypropylene or     other suitable materials, used alone or in combination. On some     embodiments, the pore size of the mesh is 200 to 500 μm. In some     embodiments, the pore size of the mesh is about 200, 250, 300, 350,     400, 450 or 500 μm. In some embodiments, the a pore size of the mesh     is 250 μm; -   iv) Repeating the maceration process with unopened flies retained in     the mesh using the dissection medium; -   v) Pooling the egg chambers by repeating filtration using a     new/clean mesh;

vi) Leaving the egg chambers to settle and removing the dissection medium. In some embodiments, the egg chambers are left to settle for 1 to 10 minutes. In some embodiments, the egg chambers are left to settle for about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 minutes. In some embodiments, the egg chambers are left to settle for 5 minutes. In some embodiments, the dissection medium is removed by decanting or aspirating with a manual pipette or a vacuum pump;

-   vii) A residual volume is left and egg chambers are transferred to     tubes. In some embodiments, the residual volume is from 50 to 150     mL. In some embodiments, the residual volume is about 50, 100, or     150 mL. In some embodiments, the residual volume is 100 mL. In some     embodiments, the tubes are conical tubes; and -   viii) Enriching the egg chambers through serial rinsing steps:     -   a) Leaving egg chambers to settle and aspirating the dissection         medium until a residual volume is left. In some embodiments, the         egg chambers are left to settle for 1 to 10 minutes. In some         embodiments, the egg chambers are left to settle for about 1, 2,         3, 4, 5, 6, 7, 8, 9, or 10 minutes. In some embodiments, the egg         chambers are left to settle for 5 minutes. In some embodiments,         the dissection medium is aspirated until 1 mL to 10 mL residual         volume is left. In some embodiments, the dissection medium is         aspirated until about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 mL         residual volume is left. In some embodiments, the dissection         medium is aspirated until 5 mL residual volume is left;     -   b) Rinsing the egg chambers by adding up to 10 to 20 mL of         dissection medium to the tubes. In some embodiments, about 11,         12, 13, 14, 15, 16, 17, 18, 19 or 20 mL of dissection medium is         added to the tubes;     -   c) Leaving the egg chambers to settle, and aspirating the         dissection medium is aspirated until an amount of dissection         medium is left. In some embodiments, the egg chambers are left         to settle for 1 to 10 minutes. In some embodiments, the egg         chambers are left to settle for about 1, 2, 3, 4, 5, 6, 7, 8, 9,         or 10 minutes. In some embodiments, the egg chambers are left to         settle for 5 minutes. In some embodiments, the dissection medium         is aspirated until 1 mL to 10 mL is left. In some embodiments,         the dissection medium is aspirated until about 1, 2, 3, 4, 5, 6,         7, 8, 9, or 10 mL is left. In some embodiments, the dissection         medium is aspirated until 1 mL is left; and     -   d) Adding clean dissection medium to the tubes and rapidly         transferring the egg chambers to a tray.         Compound Treatment

In some embodiments of the invention which relate to contacting dissected egg chambers with a compound, dissected egg chambers may be transferred to a tube after dissection. In some embodiments, the growth media containing the egg chamber may be replaced to remove dissection detritus. In some embodiments, the egg chambers are contacted with a compound while still within an ovariole, in some embodiments, the egg chambers are removed from the ovarioles and then contacted with a compound. A compound may be added to the growth media in which the egg chamber is already soaked, or may be added in new growth media which replaces the growth media which does not contain the compound. In some embodiments, the egg chamber is soaked in less than 200 μL of incubation medium. In some embodiments, the egg chamber is soaked in more than 200 μL of incubation medium. In some embodiments, the egg chamber is soaked in 200, 225, 250, 275, or 300 μL of incubation medium. The egg chamber may be soaked in growth medium which contains the compound at a temperature of 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30° C. In preferred embodiments, the egg chamber is soaked in incubation medium at a temperature of 25° C. The egg chamber may be soaked in incubation medium for a period lasting from 90 minutes to 6 hours or for a period of about 0.5, 1, 1.5, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, or 6 hours.

After an egg chamber is contacted with a compound, the egg chamber may be fixed, using chemical treatments such as paraformaldehyde, methanol, or others. Alternatively, the egg chamber may be analyzed, or processed for analysis directly, without being fixed.

In some embodiments of the invention which relate to contacting dissected egg chambers with a compound, dissected egg chambers may be transferred to several wells of a microwell plate after dissection. For example, 100-200 μL of the egg chamber/dissection medium mixture may be transferred to wells of a microwell plate. The microwell plate may have 48, 96, 384 wells or more and may or may not have an optical bottom and black, white or transparent walls. After transfer to a microwell plate, the dissection medium may be aspirated, leaving a controlled volume. In some embodiments, the controlled volume is 50 to 250 μL. In some embodiments, the controlled volume is about 50, 100, 150, 200, or 250 μL. In some embodiments, the controlled volume is 100 μL. The drug, appropriately diluted in suitable growth medium may then be added to the microwell containing the egg chambers. In some embodiments, a volume of 50-500 μL of the drug appropriately diluted in suitable growth medium is added. In some embodiments, a volume of about 50, 100, 150, 200, 250, 300, 400, or 500 μL of the drug appropriately diluted in suitable growth medium is added. In some embodiments, a volume of about 100 μL of the drug appropriately diluted in suitable growth medium is added. Non-limiting examples of suitable growth mediums are Shields and Sang M3 insect medium, Schneider's medium and others, all of which may or may not be supplemented with any combination of fetal bovine serum, serum free supplements, insulin and/or other supplements. The egg chambers may then be incubated at 20-30° C., or about 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30° C. In some embodiments, the egg chambers are incubated at 25° C. In some embodiments, incubation times may range from 1 h to 6 h. In some embodiments, the incubation time is for a period of about 0.5, 1, 1.5, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, or 6 hours. After an egg chamber is contacted with a compound, the egg chamber may be fixed, using chemical treatments such as paraformaldehyde, methanol, or others. Alternatively, the egg chamber may be analyzed, or processed for analysis directly, without being fixed. The egg chambers may be kept in the microwell plate with or without standard mountants and anti-fading products.

Some embodiments of the invention relate to contacting the egg chamber with multiple compounds at once. Therefore, the incubation medium may contain multiple compounds which are being tested for biological activity simultaneously. The use of incubation medium which contains more than one compound allows for higher throughput processes of preparing information that identifies a compound as a cancer drug candidate. In embodiments in which an egg chamber is contacted with more than one compound, and where there is a difference between the egg chamber which is contacted with more than one compound and an egg chamber not contacted with the compounds, it is necessary to subsequently test each of the compounds separately. Thus, the invention provides processes for first testing multiple compounds at once, and if a positive result is obtained in the first test, to then perform subsequent tests which evaluate each of the compounds that were tested together in the first test individually to determine which compound or compounds has biological activity or is a cancer drug candidate. In some embodiments, 2, 3, 4, 5, 6, 7, 8, 9, or 10 compounds may be tested at once in the first test.

Analysis

After an egg chamber is contacted with a compound, the egg chamber may be processed for analysis. In some embodiments, an egg chamber that has been contacted with a compound is analyzed on a slide. The egg chamber may be transferred to a slide in incubation medium. Alternatively, the incubation medium may be replaced with growth medium, so that the egg chamber is transferred to a slide in growth medium. In some embodiments, the egg chamber may be mounted in a manner suitable for observation. In some cases, egg chambers are immersed in mounting media which may or may not polymerize and may or may not contain chemical agents to reduce signal fading.

Egg chambers may be contacted with a compound at developmental stages 1 to 11 as defined in the field, e.g. in Sullivan et al., ed. Drosophila Protocols. 2000; Cold Spring Harbor Laboratory Press, ISBN 978-087969586-6; Horne-Badovinac and Bilder, 2005; and Baston and St Johnston, 2008, the contents of each of which are hereby incorporated by reference. Egg chambers may be contacted with a compound at stage 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11, or any combination thereof. Additionally, determining whether there is a difference between an egg chamber contacted with a compound, and an egg chamber not contacted with a compound may be conducted at any stage that is concurrent with, or that follows a stage in which the egg chamber is contacted with the compound.

A suitable microscope set-up may be used to score egg chambers for having healthy nurse cells or oocytes, and for differences between an egg chamber contacted with a compound and an egg chamber not contacted with the compound. In embodiments which comprise a fluorescent, phosphorescent, or otherwise luminescent label or fusion protein, microscopy may be used to determine the quantity, quality, and/or distribution of label or fusion protein in egg chambers. In some embodiments, digital images of egg chambers may be recorded. In some embodiments, digital images are recorded either by the operator or automatically using a suitable microscope and software. In some embodiments of the invention, the egg chamber is incubated, stained, or otherwise contacted with a label, such that the label becomes attached to a particular protein within the egg chamber, before analysis of the egg chamber is performed. In some embodiments, egg chambers are scored for having healthy germ cells and fluorescence quantity, quality and distribution in the apical part of the follicular epithelium using a suitable microscope set-up. Where other labeling systems are used, suitable experimental steps may be used.

In some embodiments, a positive compound is identified where healthy egg chambers have altered signal quality, quantity or distribution.

In some embodiments, identification can be made by the operator or using a suitable/tailor-made software of analysis. In some embodiments, a compound is identified to have biological activity when an egg chamber contacted with the compound has increased cell death and/or altered label or fusion protein signal quality, quantity, or distribution, compared to an egg chamber not contacted with the compound. In some embodiments, a compound is identified to be a cancer drug candidate when an egg chamber contacted with the compound does not have increased cell death, but has altered label or fusion protein signal quality, quantity, or distribution, compared to an egg chamber not contacted with the compound.

Compositions

According to another aspect of the invention, there is provided the use of a cancer drug candidate in the manufacture of a medicament for the treatment of cancer, where the medicament is formulated to deliver a dosage of the cancer drug candidate to a subject.

General techniques and compositions for making dosage forms useful in the present invention are described in the following references: 7 Modern Pharmaceutics, Chapters 9 and 10 (Banker & Rhodes, Editors, 1979); Pharmaceutical Dosage Forms: Tablets (Lieberman et al., 1981); Ansel, Introduction to Pharmaceutical Dosage Forms 2nd Edition (1976); Remington's Pharmaceutical Sciences, 17th ed. (Mack Publishing Company, Easton, Pa., 1985); Advances in Pharmaceutical Sciences (David Ganderton, Trevor Jones, Eds., 1992); Advances in Pharmaceutical Sciences Vol 7. (David Ganderton, Trevor Jones, James McGinity, Eds., 1995); Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms (Drugs and the Pharmaceutical Sciences, Series 36 (James McGinity, Ed., 1989); Pharmaceutical Particulate Carriers: Therapeutic Applications: Drugs and the Pharmaceutical Sciences, Vol 61 (Alain Rolland, Ed., 1993); Drug Delivery to the Gastrointestinal Tract (Ellis Horwood Books in the Biological Sciences. Series in Pharmaceutical Technology; J. G. Hardy, S. S. Davis, Clive G. Wilson, Eds.); Modern Pharmaceutics Drugs and the Pharmaceutical Sciences Vol. 40 (Gilbert S. Banker, Christopher T. Rhodes, Eds.). The references in their entireties are hereby incorporated by reference into this application.

This invention will be better understood by reference to the Experimental Details which follow, but those skilled in the art will readily appreciate that the specific experiments detailed are only illustrative of the invention as described more fully in the claims which follow thereafter.

EXPERIMENTAL DETAILS Example 1 Manual Soaking of Egg Chambers

Fly Culture

1-3 day-old female flies which express a fusion protein comprising Par6 fused at the C-terminus to AcGFP (Par6-AcGFP; SEQ ID NO: 11) under the control of the endogenous Par6 promoter were incubated with males for 1-2 days in bottles or vials containing fly food and yeast ad libitum. The nucleic acid sequence of Par6-AcGFP, including all “natural” control elements, is set forth as SEQ ID NO: 10.

Fly Preparation

Females were selected using a CO₂ pad, and then sacrificed by decapitation. Decapitated flies were then transferred to a dish which was kept on ice until dissection.

Dissection

The ovaries of 1-10 flies were removed for each treatment and kept in 100-200 μL growth medium. Ovarioles were carefully separated and prepared for drug treatment.

Drug Treatment

The egg-chambers were transferred to a tube and their medium, which contained dissection detritus, was removed. At least 200 μL of new growth medium containing a compound to be tested was then added for 90 minutes to 6 h. Egg chambers were then processed for analysis directly.

Mounting for Microscope Analysis

Egg chambers were mounted onto a microscope slide for observation.

Result Analysis

Suitable egg chambers (stage 7) were scored for having healthy germ cells as well as for the intensity and distribution of Par6-AcGFP in the apical part of the follicular epithelium using fluorescence microscopy. Digital images of the egg chambers were recorded.

Egg chambers that were treated with compounds and that had altered GFP signal quantity and/or distribution compared to untreated egg chambers, are those that identified the compounds with which they were contacted as being cancer drug candidates.

Example 2 Medium Scale Soaking of Egg Chambers

Purpose

Extension of the soaking of egg chambers protocol to a semi-automated format for medium scale of compound analysis.

Compounds may be routinely analyzed with medium scale soaking of egg chambers and then confirmed by low scale/manual format.

As for the low scale soaking protocol exemplified in Example 1, the medium scale soaking protocol consists of fly culture, fly preparation, dissection, drug treatment, label processing, preparation for analysis and analysis. Standard culture and preparation methods are used as described in many sources, including Theurkauf, W E, Chapter 25, Methods in Cell Biology Volume 44 (1994) Lawrence S. B. Goldstein and Eric A. Fyrberg, ISBN 978-0-12-564145-6; Ashburner, M. et al, Drosophila. A laboratory handbook. (1989), Cold Spring Harbor Laboratory Press ISBN, 0-87969-321-5 and W. Sullivan, et al., ed., Drosophila Protocols. (2000) Cold Spring Harbor Laboratory Press, ISBN 978-087969586-6, the entire contents of each of which are hereby incorporated herein by reference.

Fly Culture

-   -   1-3 day-old females are incubated with males for 1 to 2 days in         bottles/vials containing fly food and yeast ad libitum.         Fly Preparation     -   A number of female flies suitable for the number of compounds is         selected to analyze in the CO₂ pad. In one non-limiting example,         800 female flies are selected for 40 compounds.         Dissection     -   Flies are transferred to an electric liquefier filled with up to         250 mL of dissection medium. Suitable dissection mediums include         Shields and Sang M3 insect medium, Schneider's medium, Robb's         medium (Theurkauf, W E, Chapter 25, Methods in Cell Biology         Volume 44 (1994) Lawrence S. B. Goldstein and Eric A. Fyrberg,         ISBN 978-0-12-564145-6) and others, all of which may or may not         be supplemented with any combination of fetal bovine serum,         albumin and/or other supplements;     -   Egg chambers are isolated by fly maceration in the electric         liquefier with 2 second pulses repeated 3 times at low speed;     -   The fly homogenate is filtrated through a mesh placed over a         glass cup. Isolated egg chambers pass through the mesh and         unopened flies and debris are retained in the mesh. The mesh can         be made of steel, nylon, popypropylene or other suitable         materials, used alone or in combination, with a pore size of 250         μm;     -   The maceration process is repeated with unopened flies retained         in the mesh using the dissection medium;     -   Egg chambers are pooled by repeating filtration using a         new/clean mesh;     -   Egg chambers are left to settle for 5 minutes and dissection         medium is removed by decanting or aspirating with a manual         pipette or a vacuum pump;     -   A 100 mL residual volume is left and egg chambers are         transferred to conical tubes; and     -   Egg chambers are enriched through serial rinsing steps:         -   Egg chambers are left to settle for 5 minutes and dissection             medium aspirated until 5 mL residual volume is left;         -   Egg chambers are rinsed by adding up to 10-20 mL of             dissection medium to the conical tubes;         -   Egg chambers are left to settle for 5 minutes, and             dissection medium is aspirated until 1 mL is left; and         -   Clean dissection medium is added to the tubes and egg             chambers are rapidly transferred to a tray.             Drug Treatment     -   100-200 μL of the egg chamber/dissection medium mixture is         transferred to several wells of a microwell plate. The microwell         plate can have 48, 96, 384 wells or more and may or may not have         an optical bottom and black, white or transparent walls;     -   The dissection medium is aspirated, leaving a controlled volume         of 100 μL;     -   100 μL of the drug appropriately diluted in suitable growth         medium is added. Suitable growth medium include Shields and Sang         M3 insect medium, Schneider's medium and others, all of which         may or may not be supplemented with any combination of fetal         bovine serum, serum free supplements, insulin and/or other         supplements;     -   The egg chambers are incubated at 25° C. Incubation times can         range from 1 h to 6 h; and     -   Egg chambers may be fixed, using chemical treatments such as         paraformaldehyde, methanol or others, or processed directly.         Label Processing     -   Where required, egg chambers are processed using standard         procedures to detect the signal in the labeling method used.         Preparation for Analysis     -   Egg chambers are kept in the microwell with or without standard         mountants and anti-fading products.         Result Analysis     -   Suitable egg chambers (stage 1 to 11, staged as is the         convention in the field, e.g. W. Sullivan, et al., ed.,         Drosophila Protocols. (2000) Cold Spring Harbor Laboratory         Press, ISBN 978-087969586-6) are scored for having healthy germ         cells and fluorescence quantity, quality and distribution in the         apical part of the follicular epithelium using a suitable         microscope set-up. Where other labeling systems are used,         suitable experimental steps are used.     -   Digital images are recorded either by the operator or         automatically using a suitable microscope and software.     -   A positive compound is identified where healthy egg chambers         have altered signal quality, quantity or distribution.         Identification can be made by the operator or using a         suitable/tailor-made software of analysis.

Example 3 Injection of Embryos

Fly Preparation

2-3 day-old flies which express Par6-AcGFP under the control of the endogenous Par6 promoter and an apple juice/agar substrate plate are used to prepare pots for egg laying. Flies are allowed to adapt to the pots for a minimum of 24 h.

Embryo Laying

On the day of the experiment, the first apple juice/agar substrate plate is replaced with a second apple juice/agar substrate plate. After 1 h the second apple juice/agar substrate plate is replaced with another apple juice/agar substrate plate which is used to collect additional embryos. Apple juice/agar substrate plates are continuously replaced as more embryos were collected each hour until the desired number of embryos are collected. Once an apple juice/agar substrate plate containing embryos is removed, it is incubated at 25° C. for 50-60 minutes.

Embryo Harvesting and Alignment

A basket strainer is placed in a petri dish which is contains 0.1% Tween-2/H₂O. Each embryo is then harvested from the apple juice/agar plate with a paint brush that is wet with 0.1% Tween-20/H₂O and then added to the basket. The 0.1% Tween-20/H₂O in the petri dish is then discarded and replaced with 50% bleach in H₂O to remove the chorions of embryos in the basket. The embryos are incubated in the 50% bleach solution for about 1.5 minutes, after which they are washed by replacing the 50% bleach solution with H₂O. The H₂O is replaced with new H₂O at least 4 times to wash the embryos. The basket strainer is then removed from the petri dish, and the bottom of the basket is dried with paper to facilitate removal of the embryos with a spatula. The embryos are then placed on a small piece of agar and about 50 embryos are aligned with their posterior poles pointing in the same direction. A slide is prepared with tape and aligned over the embryos so that they stick to the tape. The embryos are then desiccated for 4 minutes at 25° C. in a petri dish which has been filled with silica gel.

Injection of Embryos

A needle that comes to a closed point at its tip is filled with a solution comprising a compound to be tested for biological activity, and the tip of the needle is broken to provide an opening through which the solution may be injected. The drop size of the solution which exits the needle during each injection is adjusted with a graticle in order to be about 420 pL of solution. The embryos are then injected through their posterior poles.

Analysis

Development of the treated embryos is followed for up to 4 h, and they are scored for developmental differences, cellularization differences and altered amounts of cell death compared to untreated embryos. The AcGFP signal in the embryos is traced for location and intensity.

Results

Embryos that are treated with compounds and that have altered GFP signal quantity and/or distribution compared to untreated embryos are those that identify the compounds with which they were injected as being cancer drug candidates.

Example 4 Cancer Drug Candidate Validation

Compounds that are identified as cancer drug candidates using processes of the invention are evaluated for efficacy in appropriate mammalian models. Compounds identified as cancer drug candidates using the process described in Example 1, 2, or 3 are administered to groups of mice, which each have a carcinoma. Mice are treated with the drug candidates until they are sacrificed for analysis or die from the carcinoma. A proportion of the cancer drug candidates which are tested in vivo are found to effectively inhibit tumor growth in the mice. Furthermore, a proportion of the cancer drug candidates are found to effectively inhibit cancer cell survival in the Additionally, a proportion of the cancer drug candidates are found to effectively inhibit cancer metastasis in the mice.

When cancer drug candidates identified using the process described in Example 1, 2, or 3 are compared to cancer drug candidates identified using in vitro processes, the proportion of the cancer drug candidates which are effective at inhibiting tumor growth while being well tolerated in mice is greater for those identified using the process described in Example 1, 2, or 3 than those identified using an analogous in vitro screening process. Additionally, the proportion of the cancer drug candidates which are effective at killing cancer cells while being well tolerated in mice is greater for those identified using the process in Example 1, 2, or 3 than those identified using an analogous in vitro screening process. Furthermore, the proportion of the cancer drug candidates which are effective at reducing the metastasis cancer cells while being well tolerated in mice is greater for those identified using the process in Example 1, 2, or 3, than those identified using an analogous in vitro screening process.

When cancer drug candidates identified using the process described in Example 1, 2, and 3 are compared to cancer drug candidates identified using an analogous in vivo process which uses a D. melanogaster which was genetically modified to have the reduced or increased function of a protein (“traditional Drosophila screening process”), the proportion of the cancer drug candidates which are effective at inhibiting tumor growth while being well tolerated in mice is greater for those identified using the process described in Example 1, 2, and 3 than those identified using an analogous traditional Drosophila screening process. Additionally, the proportion of the cancer drug candidates which are effective at killing cancer cells while being well tolerated in mice is greater for those identified using the process in Example 1, 2, or 3 than those identified using an analogous traditional Drosophila screening process. Furthermore, the proportion of the cancer drug candidates which are effective at reducing the metastasis cancer cells while being well tolerated in mice is greater for those identified using the process in Example 1, 2, or 3, than those identified using an analogous traditional Drosophila screening process.

Discussion

The invention provides screening processes that identify cancer drug candidates with lower background effects and higher reliability than other D. melanogaster-based screening processes. One advantageous aspect of the subject invention is that the D. melanogaster embryos and egg chambers of the invention are minimally genetically modified. The D. melanogaster embryos and egg chambers of the invention are wild-type with the exception that they may express a reporter polypeptide fused to an endogenous protein. Aspects of the invention do not rely on mutants or flies that are modified to have the significant gain or loss of function of any gene, and therefore their cells behave normally. The approaches disclosed herein allow for cleaner, more reliable cancer drug candidate identification than other D. melanogaster-based screens.

The D. melanogaster Egg Chamber

Oogenesis requires many cellular processes, including cell cycle control, cell fate specification, cell polarization, and epithelial morphogenesis (Bastock and St Johnston, 2008). The Drosophila egg chamber comprises both germ and somatic cells which signal to each other and undergo profound cellular changes throughout oogenesis. Many of the morphological changes observed during oogenesis occur in the follicular epithelium, the portion of the egg chamber which produces yolk and eggshell components of the egg, and which also signals to the germ cells to help determine future embryonic axes (Horne-Badovinac and Bilder, 2005). Surprisingly, as disclosed herein, a compound's effects on cellular processes observed within the D. melanogaster egg chamber are a reliable predictor of the compound's ability to perturb cancer cell proliferation, metastasis, and survival in mammals.

Par6

Par6 regulates cell polarity and fate determination during egg chamber and embryonic development in D. melanogaster (Petronczki and Knoblich, 2000). As a PB1 domain protein that links aPKCs to Rac1, Par6, has been suggested to play a role in oncogenic PKCι signaling (Fields et al. 2007; Brumby and Richardson, 2005). Fields et al. 2007 purported to describe in vitro screens for compounds which disrupt the interaction of the PB1-PB1 domain interaction between PKCι and Part, however, Fields et al. did not teach or suggest conducting in vivo drug screens which employed Part in any capacity, in D. melanogaster or otherwise. Furthermore, aspects of the subject invention relate to the identification of cancer drug candidates that alter Par6 function or expression in cells that behave normally within an in vivo context. Surprisingly, the ability of a compound to directly or indirectly alter the normal expression and/or function of Par6, or the behavior of cells that express Par6 within the epithelium of an almost completely wild-type D. melanogaster embryo or egg chamber identifies that compound as a cancer drug candidate.

REFERENCES

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What is claimed is:
 1. A process for identifying whether a compound is an epithelial cancer drug candidate comprising: i) obtaining, by dissection from at least one D. melanogaster adult female fly, at least one D. melanogaster egg chamber which is genetically unmodified except that the at least one D. melanogaster egg chamber comprises at least one nucleotide sequence encoding a Par6 fusion protein under control of the Par6 endogenous promoter, wherein the Par6 fusion protein comprises a reporter polypeptide fused to Par6, and wherein the nucleic acid sequence that encodes the Par6 fusion protein and the Par6 endogenous promoter is SEQ ID NO: 10; ii) contacting the at least one dissected egg chamber with the compound by soaking it in an incubation medium containing the compound; and iii) comparing the level of expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound, to the level in the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound, wherein the presence of a difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound identifies the compound as an epithelial cancer drug candidate.
 2. The process of claim 1, wherein the difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the apical part of the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound comprises increased or decreased expression.
 3. The process of claim 1, wherein the difference in the expression of the Par6 fusion protein in the apical part the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the apical part of the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound comprises a different localization of the Par6 fusion protein within follicle epithelial cells.
 4. The process of claim 3, wherein there is proportionally less localization of the Par6 fusion protein at the apical side of the follicle epithelial cells of the at least one dissected egg chamber contacted with the compound compared to the follicle epithelial cells of the corresponding at least one dissected egg chamber not contacted with the compound.
 5. The process of claim 1, wherein difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the apical part of the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound comprises a different location of protein production or post-transcriptional modification of the Par6 fusion protein.
 6. A process for identifying whether a compound is an epithelial cancer drug candidate comprising: (a) i) obtaining, by dissection from at least one D. melanogaster adult female fly, at least one D. melanogaster egg chamber which is genetically unmodified except that the at least one D. melanogaster egg chamber comprises at least one nucleotide sequence encoding a Par6 fusion protein under control of the Par6 endogenous promoter, wherein the Par6 fusion protein comprises a reporter polypeptide fused to Par6, wherein the nucleic acid sequence that encodes the Par6 fusion protein and the Par6 endogenous promoter is SEQ ID NO: 10; ii) contacting the at least one dissected egg chamber with the compound, and up to four additional compounds by soaking it in an incubation medium containing the compounds; iii) comparing the level of expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound and up to four additional compounds, to the level in the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound and up to four additional compounds; iv) if there is a difference in the expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound and up to four additional compounds compared to the apical part of the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound, contacting at least one additional dissected egg chamber according to step i) with the compound but not the additional compound or compounds of step ii) and step iii); and v) determining whether there is a difference in the expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one additional dissected egg chamber of step iv) and the apical part of the follicular epithelium of a corresponding at least one additional dissected egg chamber not contacted with the compound, wherein the presence of a difference in the expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one additional dissected egg chamber of iv) compared to the apical part of the follicular epithelium of the corresponding at least one additional dissected egg chamber not contacted with the compound identifies the compound as an epithelial cancer drug candidate; or (b) i) obtaining, by dissection from at least one D. melanogaster adult female fly, at least one D. melanogaster egg chamber which is genetically unmodified except that the at least one D. melanogaster egg chamber optionally comprises at least one nucleotide sequence encoding a Par6 fusion protein under control of the Par6 endo endogenous promoter, wherein the Par6 fusion protein comprises a reporter polypeptide fused to Par6, wherein the nucleic acid sequence that encodes the Par6 fusion protein and the Par6 endogenous promoter is SEQ ID NO: 10; ii) contacting the at least one dissected egg chamber with the compound by soaking it in an incubation medium containing the compound; iii) comparing the level of expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound, to the level in the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound; and iv) observing whether there is substantially more toxicity among cells other than follicle cells of the at least one dissected egg chamber contacted with the compound than in the corresponding at least one dissected egg chamber not contacted with the compound, wherein the presence of a difference in expression of the reporter polypeptide in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound, without the presence of substantially more toxicity among cells other than follicle cells of the at least one dissected egg chamber contacted with the compound compared to the corresponding at least one dissected egg chamber not contacted with the compound, identifies the compound as an epithelial cancer drug candidate.
 7. The process of claim 1, wherein at least 10, 15, 20, 25, or 50 dissected D. melanogaster egg chambers are obtained and contacted with the compound.
 8. A process for producing an epithelial cancer drug comprising: (a) i) preparing or obtaining a group of compounds to be screened; ii) performing the process of claim 1 for each compound from the group of compounds to identify an epithelial cancer drug candidate; and iii) producing the compound identified in step ii), thereby producing the epithelial cancer drug, or (b) i) obtaining, by dissection from at least one D. melanogaster adult female fly, at least one D. melanogaster egg chamber which is genetically unmodified except that the at least one D. melanogaster egg chamber comprises at least one nucleotide sequence encoding a Par6 fusion protein under control of the Par6 endogenous promoter, wherein the Par6 fusion protein comprises a reporter polypeptide fused to Par6, and wherein the nucleic acid sequence that encodes the Par6 fusion protein and the Par6 endogenous promoter is SEQ ID NO: 10; ii) contacting the at least one dissected egg chamber with the compound by soaking it in an incubation medium containing the compound; iii) comparing the level of expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound, to the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound, wherein the presence of a difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound identifies the compound as an epithelial cancer drug; and iv) producing the compound identified in step iii), thereby producing the epithelial cancer drug, or (c) i) obtaining, by dissection from at least one D. melanogaster adult female fly, at least one D. melanogaster egg chamber which is genetically unmodified except that the at least one D. melanogaster egg chamber optionally comprises at least one nucleotide sequence encoding a Par6 fusion protein under control of the Par6 endogenous promoter, wherein the Par6 fusion protein comprises a reporter polypeptide fused to Par6, and wherein the nucleic acid sequence that encodes the Par6 fusion protein and the Par6 endogenous promoter is SEQ ID NO: 10; ii) contacting the at least one dissected egg chamber with the compound, and up to four additional compounds by soaking it in an incubation medium containing the compounds; iii) comparing the level of expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound and up to four additional compounds, to the level in the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound and up to four additional compounds; iv) if there is a difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound and up to four additional compounds compared to the follicular epithelium of the corresponding at least one dissected egg chamber not contacted with the compound, contacting at least one additional dissected egg chamber according to step i) with the compound but not the additional compound or compounds of step ii) and step iii); and v) comparing the level of expression or the Par6 fusion protein in the apical part of the follicular epithelium of the at least one additional dissected egg chamber of step iv), to the level in the apical part of the follicular epithelium of the corresponding at least one additional dissected egg chamber not contacted with the compound, wherein the presence of a difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one additional dissected egg chamber of step iv) compared to the apical part of the follicular epithelium of the corresponding at least one additional dissected egg chamber not contacted with the compound identifies the compound as an epithelial cancer drug; and vi) producing the compound identified in step v), thereby producing the epithelial cancer drug.
 9. The process of claim 1, wherein the at least one dissected egg chamber is soaked in the incubation medium containing the compound when the at least one dissected egg chamber is at a stage other than stage 1, 2, 3, or
 4. 10. The process of claim 9, wherein the at least one dissected egg chamber is soaked in the incubation medium containing the compound when the at least one dissected egg chamber is at stage
 7. 11. The process of claim 1, wherein the difference in the expression of the Par6 fusion protein in the apical part of the follicular epithelium of the at least one dissected egg chamber contacted with the compound compared to the expression of the Par6 fusion protein in the apical part of the follicular epithelium of a corresponding at least one dissected egg chamber not contacted with the compound is observed in a border cell, a stretch cell, a polar cell, or a centripetal cell using a microscope.
 12. The process of claim 1, wherein the epithelial cancer comprises cells with disrupted Par6 function or disrupted epithelial cell polarity. 